Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase - Test2 - elhamkhani - TriplyDB

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

http://www.wikidata.org/entity/Q33842154

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)Control of Appetite and Food Preference by NMDA Receptor and Its Co-Agonist d-Serine Chronic Glutamate Toxicity in Neurodegenerative Diseases-What is the Evidence?Peroxisomes in brain development and function State of play in amyotrophic lateral sclerosis genetics Sumoylation of critical proteins in amyotrophic lateral sclerosis: emerging pathways of pathogenesis The role of D-serine and glycine as co-agonists of NMDA receptors in motor neuron degeneration and amyotrophic lateral sclerosis (ALS)Naturally occurring genetic variability in expression of Gsta4 is associated with differential survival of axotomized rat motoneurons Cell-type specific mechanisms of D-serine uptake and release in the brain A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK Activity of D-amino acid oxidase is widespread in the human central nervous system.Heterogeneity of D-Serine Distribution in the Human Central Nervous System.Role of mitochondria in mutant SOD1 linked amyotrophic lateral sclerosis The role of D-amino acids in amyotrophic lateral sclerosis pathogenesis: a review.Genetic heterogeneity of amyotrophic lateral sclerosis: implications for clinical practice and research.Understanding the role of TDP-43 and FUS/TLS in ALS and beyond.D-amino acid oxidase controls motoneuron degeneration through D-serine.Adaptive evolution and elucidating the potential inhibitor against schizophrenia to target DAOA (G72) isoforms.Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations.Paradoxical roles of serine racemase and D-serine in the G93A mSOD1 mouse model of amyotrophic lateral sclerosis.D-Serine Production, Degradation, and Transport in ALS: Critical Role of Methodology Understanding renal nuclear protein accumulation: an in vitro approach to explain an in vivo phenomenon.Production of hydrogen sulfide from d-cysteine and its therapeutic potential.Genetics of amyotrophic lateral sclerosis: an update.Clinical neurogenetics: amyotrophic lateral sclerosis.The C-terminal region of G72 increases D-amino acid oxidase activity.Sequestosome-1 (SQSTM1) sequence variants in ALS cases in the UK: prevalence and coexistence of SQSTM1 mutations in ALS kindred with PDB.Characterization of chiral amino acids from different milk origins using ultra-performance liquid chromatography coupled to ion-mobility mass spectrometry.Dysregulation of axonal transport and motorneuron diseases.Emerging drugs for amyotrophic lateral sclerosis.Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia.Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis.Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology.D-Amino acids in the brain and mutant rodents lacking D-amino-acid oxidase activity.The genetics and neuropathology of amyotrophic lateral sclerosis.Amyotrophic lateral sclerosis: an update on recent genetic insights.Vitamin D as a potential therapy in amyotrophic lateral sclerosis.RNA metabolism in ALS: when normal processes become pathological.Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges.

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P2860

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

http://www.wikidata.org/entity/Q33842154

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2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Familial amyotrophic lateral s ...... tation in D-amino acid oxidase

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Familial amyotrophic lateral s ...... tation in D-amino acid oxidase

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Familial amyotrophic lateral s ...... tation in D-amino acid oxidase

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Familial amyotrophic lateral s ...... tation in D-amino acid oxidase

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Familial amyotrophic lateral s ...... tation in D-amino acid oxidase

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Familial amyotrophic lateral s ...... tation in D-amino acid oxidase

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Proceedings of the National Academy of Sciences of the United States of America

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Familial amyotrophic lateral s ...... tation in D-amino acid oxidase

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Alex Morris

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Han-Jou Chen

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James Habgood

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John Mitchell

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Miles Payling

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Nicholas D Mazarakis

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Praveen Paul

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Sabine Winkler

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Stefania Panoutsou

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P2860

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

Induction of serine racemase by inflammatory stimuli is dependent on AP-1

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

Active site plasticity in D-amino acid oxidase: a crystallographic analysis

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Serine racemase: a glial enzyme synthesizing D-serine to regulate glutamate-N-methyl-D-aspartate neurotransmission

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107

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Jacqueline de Belleroche

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2010-04-05T00:00:00Z

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43023388

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amyotrophic lateral sclerosis

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